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URLhttps://doi.org/10.18429/JACoW-IPAC2025-TUPB046
TitleDesign of a helium ion linear accelerator for astatine production
Authors
  • M. Vretenar, A. Lombardi, L. Nikitovic
    European Organization for Nuclear Research
AbstractAstatine 211 is one of the most effective theragnostics isotopes for targeted alpha therapy of cancer. Connected to a carrier that links to cancer cells when injected in a patient, this powerful alpha emitter can selectively destroy cancerous cells. Accelerator production of 211At requires sending beams of fully stripped helium ions (alpha particles) on a bismuth target at the energy of 7.1 Me/u. To obtain sufficient doses for hospital production of 211At, currents higher than what provided by cyclotrons are required. For this type of particle and intensities, cyclotrons are limited by the large amount of beam loss and activation in the extraction region, while linacs are virtually loss-free and much better suited for At production. The design of an innovative linac for At production is presented, based on an alpha particle source of new design, a compact Radio Frequency Quadrupole, and a Quasi-Alvarez Drift Tube Linac (QA-DTL) going up to the final energy. Thanks to the QA-DTL low injection energy and compact design, the linac is only 10 meters in length. The overall design is presented, together with detailed RF and beam optics simulations.
Paperdownload: TUPB046.pdf
CiteBibTeX, LaTeX, Text/Word, RIS, EndNote
Conference16th International Particle Accelerator Conference
Series
LocationTaipei, Taiwan
Date01-06 Jun 2025
PublisherJACoW Publishing, Geneva, Switzerland
Editorial Board* Ming-Chyuan Lin - National Synchrotron Radiation Research Center * Yoichi Sato - KEK * Jui-Che Huang - National Synchrotron Radiation Research Center * David Button - Australian Nuclear Science and Technology Organisation * Ping-Shun Chuang - National Synchrotron Radiation Research Center
Online ISBN978-3-95450-248-6
Online ISSN2673-5490
Received28 May 2025
Revised05 June 2025
Accepted13 October 2025
Issued05 November 2025
DOI10.18429/JACoW-IPAC2025-TUPB046
Pages1067-1070